Canonical Allele Identifier: PA095733
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2081
ClinVar RCV Id: RCV000002162 RCV000724276
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Tyr295His
CA252094
NM_000159.4:c.883T>C